PL203960B1 - Sposób wytwarzania elementu żelowego - Google Patents

Sposób wytwarzania elementu żelowego

Info

Publication number: PL203960B1
Authority: PL; Poland
Prior art keywords: perfume; premix; liquid polymer; premixture; polymer
Prior art date: 2001-10-16

Application number

PL368339A

Other languages

English (en)

Polish (pl)

Other versions

PL368339A1 (en

Inventor

Nicholas O'leary

Geraldine Lang

Original Assignee

Reckitt Benckiser Uk Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2001-10-16

Filing date

2002-10-09

Publication date

2009-11-30

2002-10-09 Application filed by Reckitt Benckiser Uk Ltd filed Critical Reckitt Benckiser Uk Ltd

2005-03-21 Publication of PL368339A1 publication Critical patent/PL368339A1/xx

2009-11-30 Publication of PL203960B1 publication Critical patent/PL203960B1/pl

Links

238000004519 manufacturing process Methods 0.000 title claims abstract description 19
239000002304 perfume Substances 0.000 claims abstract description 92
229920000642 polymer Polymers 0.000 claims description 68
239000004971 Cross linker Substances 0.000 claims description 50
239000007788 liquid Substances 0.000 claims description 50
239000004615 ingredient Substances 0.000 claims description 48
239000000203 mixture Substances 0.000 claims description 44
239000000499 gel Substances 0.000 claims description 34
238000000034 method Methods 0.000 claims description 32
239000003431 cross linking reagent Substances 0.000 claims description 16
150000001299 aldehydes Chemical class 0.000 claims description 14
150000004985 diamines Chemical class 0.000 claims description 10
150000002576 ketones Chemical class 0.000 claims description 10
238000002156 mixing Methods 0.000 claims description 9
239000005062 Polybutadiene Substances 0.000 claims description 8
229920002857 polybutadiene Polymers 0.000 claims description 8
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical group CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 5
150000008064 anhydrides Chemical group 0.000 claims description 5
239000000758 substrate Substances 0.000 claims description 5
239000002386 air freshener Substances 0.000 claims description 3
229920001195 polyisoprene Polymers 0.000 claims description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
125000000524 functional group Chemical group 0.000 description 17
239000003205 fragrance Substances 0.000 description 12
239000011521 glass Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
125000003277 amino group Chemical group 0.000 description 5
150000001298 alcohols Chemical class 0.000 description 4
IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 description 4
HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 4
239000000796 flavoring agent Substances 0.000 description 4
235000019634 flavors Nutrition 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
150000003138 primary alcohols Chemical class 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 3
KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
230000000295 complement effect Effects 0.000 description 3
238000004132 cross linking Methods 0.000 description 3
150000002466 imines Chemical class 0.000 description 3
150000003141 primary amines Chemical class 0.000 description 3
239000000126 substance Substances 0.000 description 3
FINOAUDUYKVGDS-UHFFFAOYSA-N (2-tert-butylcyclohexyl) acetate Chemical compound CC(=O)OC1CCCCC1C(C)(C)C FINOAUDUYKVGDS-UHFFFAOYSA-N 0.000 description 2
RCSBILYQLVXLJG-UHFFFAOYSA-N 2-Propenyl hexanoate Chemical compound CCCCCC(=O)OCC=C RCSBILYQLVXLJG-UHFFFAOYSA-N 0.000 description 2
JRJBVWJSTHECJK-PKNBQFBNSA-N 3-Methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one Chemical compound CC(=O)C(\C)=C\C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-PKNBQFBNSA-N 0.000 description 2
WWJLCYHYLZZXBE-UHFFFAOYSA-N 5-chloro-1,3-dihydroindol-2-one Chemical compound ClC1=CC=C2NC(=O)CC2=C1 WWJLCYHYLZZXBE-UHFFFAOYSA-N 0.000 description 2
239000009261 D 400 Substances 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
KGEKLUUHTZCSIP-UHFFFAOYSA-N Isobornyl acetate Natural products C1CC2(C)C(OC(=O)C)CC1C2(C)C KGEKLUUHTZCSIP-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
241000721662 Juniperus Species 0.000 description 2
235000019502 Orange oil Nutrition 0.000 description 2
DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 2
DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 2
239000001940 [(1R,4S,6R)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Substances 0.000 description 2
125000003158 alcohol group Chemical group 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000010636 coriander oil Substances 0.000 description 2
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
XSNQECSCDATQEL-UHFFFAOYSA-N dihydromyrcenol Chemical compound C=CC(C)CCCC(C)(C)O XSNQECSCDATQEL-UHFFFAOYSA-N 0.000 description 2
229930008394 dihydromyrcenol Natural products 0.000 description 2
235000013399 edible fruits Nutrition 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000010642 eucalyptus oil Substances 0.000 description 2
229940044949 eucalyptus oil Drugs 0.000 description 2
239000010648 geranium oil Substances 0.000 description 2
235000019717 geranium oil Nutrition 0.000 description 2
239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
239000010502 orange oil Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000010668 rosemary oil Substances 0.000 description 2
229940058206 rosemary oil Drugs 0.000 description 2
239000007787 solid Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
150000003505 terpenes Chemical class 0.000 description 2
235000007586 terpenes Nutrition 0.000 description 2
VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 2
235000013769 triethyl citrate Nutrition 0.000 description 2
239000001069 triethyl citrate Substances 0.000 description 2
JJWWUTCHOAKZPR-UHFFFAOYSA-N 4-methylpent-4-en-2-yl 2-methylpropanoate Chemical compound CC(C)C(=O)OC(C)CC(C)=C JJWWUTCHOAKZPR-UHFFFAOYSA-N 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
229920013646 Hycar Polymers 0.000 description 1
241000949440 Nanger dama Species 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
VWTINHYPRWEBQY-UHFFFAOYSA-N denatonium Chemical compound [O-]C(=O)C1=CC=CC=C1.C=1C=CC=CC=1C[N+](CC)(CC)CC(=O)NC1=C(C)C=CC=C1C VWTINHYPRWEBQY-UHFFFAOYSA-N 0.000 description 1
230000001877 deodorizing effect Effects 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
239000000975 dye Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000012530 fluid Substances 0.000 description 1
229920001002 functional polymer Polymers 0.000 description 1
238000001879 gelation Methods 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
150000005673 monoalkenes Chemical class 0.000 description 1
ATBNMWWDBWBAHM-UHFFFAOYSA-N n-decyl-n-methyldecan-1-amine Chemical compound CCCCCCCCCCN(C)CCCCCCCCCC ATBNMWWDBWBAHM-UHFFFAOYSA-N 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
150000003333 secondary alcohols Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1
125000006850 spacer group Chemical group 0.000 description 1
150000003509 tertiary alcohols Chemical class 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
- A61L9/04—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
- A61L9/12—Apparatus, e.g. holders, therefor
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
- A61L9/04—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
- A61L9/048—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating air treating gels

Landscapes

Health & Medical Sciences (AREA)
Epidemiology (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Fats And Perfumes (AREA)
Compositions Of Macromolecular Compounds (AREA)
Detergent Compositions (AREA)
Cosmetics (AREA)
Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)

PL368339A 2001-10-16 2002-10-09 Sposób wytwarzania elementu żelowego PL203960B1 (pl)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB0124728A GB2381001B (en)	2001-10-16	2001-10-16	Process for preparing a perfumed gel

Publications (2)

Publication Number	Publication Date
PL368339A1 PL368339A1 (en)	2005-03-21
PL203960B1 true PL203960B1 (pl)	2009-11-30

Family

ID=9923861

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL368339A PL203960B1 (pl)	2001-10-16	2002-10-09	Sposób wytwarzania elementu żelowego

Country Status (15)

Country	Link
US (1)	US7132461B2 (de)
EP (1)	EP1436017B1 (de)
CN (1)	CN1292800C (de)
AR (1)	AR036886A1 (de)
AT (1)	ATE314100T1 (de)
AU (1)	AU2002330625B2 (de)
BR (1)	BR0213307B1 (de)
CA (1)	CA2464345C (de)
DE (1)	DE60208409T2 (de)
ES (1)	ES2256532T3 (de)
GB (1)	GB2381001B (de)
MX (1)	MXPA04003601A (de)
PL (1)	PL203960B1 (de)
WO (1)	WO2003033038A1 (de)
ZA (1)	ZA200403125B (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7393905B2 (en) *	2004-12-29	2008-07-01	Weyerhaeuser Company	Crosslinked mixed carboxylated polymer network
EP1872767A1 (de) *	2006-06-30	2008-01-02	Ernst Mühlbauer GmbH & Co.KG	Polymerisierbares Dentalmaterial
US20080015295A1 (en) *	2006-07-11	2008-01-17	Williams Virgil Ag	Polymeric gel composition and method for making
JP2010516862A (ja)	2007-02-15	2010-05-20	ザプロクターアンドギャンブルカンパニー	有益剤送達組成物
US7700665B2 (en) *	2007-12-06	2010-04-20	Orlandi Inc.	Fragrant gel polymer system
WO2010014807A2 (en) *	2008-08-01	2010-02-04	The Procter & Gamble Company	Perfume compositions comprising functional perfume components
US20130338056A1 (en)	2010-07-08	2013-12-19	Sven Dobler	Fragrant gel polymer with solvents
US8877139B2 (en)	2010-08-13	2014-11-04	The Procter & Gamble Company	Compositions comprising a functional perfume component mixture

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0728021B2 (de) *	1994-08-19	2008-03-05	Reckitt Benckiser (UK) LIMITED	Parfümierungsvorrichtung zum parfümieren und sanieren von umgebungsluft
CN1217214A (zh) *	1997-11-17	1999-05-26	淄博美华化工有限公司	水性固体状空气清新剂
DE69908796T2 (de) *	1998-10-22	2004-04-01	Reckitt Benckiser (Uk) Limited, Slough	Dampffreisetzender gegenstand
GB2363717B (en) *	2000-04-19	2002-06-19	Reckitt Benckiser	Coloured anhydrous gel element

2001
- 2001-10-16 GB GB0124728A patent/GB2381001B/en not_active Expired - Fee Related
2002
- 2002-10-09 ES ES02767697T patent/ES2256532T3/es not_active Expired - Lifetime
- 2002-10-09 DE DE60208409T patent/DE60208409T2/de not_active Expired - Lifetime
- 2002-10-09 MX MXPA04003601A patent/MXPA04003601A/es active IP Right Grant
- 2002-10-09 CA CA2464345A patent/CA2464345C/en not_active Expired - Fee Related
- 2002-10-09 US US10/492,807 patent/US7132461B2/en not_active Expired - Lifetime
- 2002-10-09 EP EP02767697A patent/EP1436017B1/de not_active Expired - Lifetime
- 2002-10-09 CN CNB028204646A patent/CN1292800C/zh not_active Expired - Fee Related
- 2002-10-09 AT AT02767697T patent/ATE314100T1/de not_active IP Right Cessation
- 2002-10-09 PL PL368339A patent/PL203960B1/pl unknown
- 2002-10-09 WO PCT/GB2002/004583 patent/WO2003033038A1/en not_active Ceased
- 2002-10-09 AU AU2002330625A patent/AU2002330625B2/en not_active Ceased
- 2002-10-09 BR BRPI0213307-5A patent/BR0213307B1/pt not_active IP Right Cessation
- 2002-10-16 AR ARP020103887A patent/AR036886A1/es not_active Application Discontinuation
2004
- 2004-04-23 ZA ZA200403125A patent/ZA200403125B/en unknown

Also Published As

Publication number	Publication date
DE60208409T2 (de)	2006-09-07
MXPA04003601A (es)	2004-07-30
CA2464345A1 (en)	2003-04-24
GB0124728D0 (en)	2001-12-05
WO2003033038A1 (en)	2003-04-24
ZA200403125B (en)	2005-07-27
BR0213307B1 (pt)	2014-12-30
GB2381001A (en)	2003-04-23
ATE314100T1 (de)	2006-01-15
CN1571681A (zh)	2005-01-26
EP1436017A1 (de)	2004-07-14
EP1436017B1 (de)	2005-12-28
DE60208409D1 (de)	2006-02-02
PL368339A1 (en)	2005-03-21
AR036886A1 (es)	2004-10-13
US20050043432A1 (en)	2005-02-24
US7132461B2 (en)	2006-11-07
AU2002330625B2 (en)	2006-11-30
BR0213307A (pt)	2004-10-13
GB2381001B (en)	2003-11-26
CA2464345C (en)	2011-05-24
CN1292800C (zh)	2007-01-03
ES2256532T3 (es)	2006-07-16

Legal Events

Date	Code	Title	Description
2010-10-29	RECP	Rectifications of patent specification

Publication	Publication Date	Title
KR100400116B1 (ko)	2003-12-31	주위공기또는폐쇄공간의방향,탈취또는청정용제품및이의방향,탈취또는청정방법
US4734278A (en)	1988-03-29	Perfumed polymeric resin essentially consisting of a polyether-esteramide
JPH11511497A (ja)	1999-10-05	安定な布帛柔軟剤組成物
MXPA06013734A (es)	2007-08-14	Composiciones y articulos que contienen una matriz de polimero entrelazado y un liquido activo inmovilizado, asi como metodos para producir y utilizar las mismas.
CN1216650C (zh)	2005-08-31	有色无水凝胶成分
US6846491B1 (en)	2005-01-25	Clear, polymeric gel composition and method for producing the same
PL203960B1 (pl)	2009-11-30	Sposób wytwarzania elementu żelowego
AU2002330625A1 (en)	2003-07-03	A process for preparing a gel element
US20080015295A1 (en)	2008-01-17	Polymeric gel composition and method for making
JP4686040B2 (ja)	2011-05-18	ゲル状芳香剤組成物
JP4791143B2 (ja)	2011-10-12	透明ゲル化剤組成物、透明ゲルおよび透明ゲルの製造方法
KR100817235B1 (ko)	2008-03-27	유성겔 방향제 조성물
JP2003003029A (ja)	2003-01-08	水性ゲル状芳香剤用組成物及び水性ゲル状芳香剤
JP2003290331A (ja)	2003-10-14	ゲル状芳香・消臭剤組成物
JPS6363231B2 (de)	1988-12-06
GB2363717A (en)	2002-01-09	Homogenously coloured gels for perfuming/deodorising air comprising cross linked polymer & metal-free solvent dye compatible with the perfume/deodorising base
WO2016112262A1 (en)	2016-07-14	Polymeric gel composition for fragrancing and fabric treatment in a clothes dryer